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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K223812
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Sensis Vibe Hemo 2 01/09/2024 FEI # 2240869
Siemens Medical Solutions USA, Inc
Sensis Vibe systems with software version VD15B-Intended to be used as a diagnostic and administrati... 2 07/25/2024 FEI # 2240869
Siemens Medical Solutions USA, Inc
Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended... 2 07/25/2024 FEI # 2240869
Siemens Medical Solutions USA, Inc
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